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Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine
OBJECTIVES: Meta-analysis based on individual patient data (IPD) from randomised trials is superior to using published summary data since it facilitates subgroup and multiple variable analyses. Guidelines and funders expect that researchers share IPD for bona fide analyses, but in practice, this is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482449/ https://www.ncbi.nlm.nih.gov/pubmed/32912955 http://dx.doi.org/10.1136/bmjopen-2020-038765 |
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author | Scutt, Polly Woodhouse, Lisa J Montgomery, Alan A Bath, Philip M |
author_facet | Scutt, Polly Woodhouse, Lisa J Montgomery, Alan A Bath, Philip M |
author_sort | Scutt, Polly |
collection | PubMed |
description | OBJECTIVES: Meta-analysis based on individual patient data (IPD) from randomised trials is superior to using published summary data since it facilitates subgroup and multiple variable analyses. Guidelines and funders expect that researchers share IPD for bona fide analyses, but in practice, this is done variably. Here, we report the experience of obtaining IPD for two collaborative analysis studies. SETTING: Two linked studies required IPD from published randomised trials. The leading researchers for eligible trials were approached and asked to share IPD including trial characteristics, patient demographics, baseline clinical data and outcome measures. PARTICIPANTS: Participants in eligible randomised controlled trials included patients with or at risk of cognitive decline/vascular events. PRIMARY AND SECONDARY OUTCOME MEASURES: Numbers (%) of trials where the leading researcher responded favourably/negatively or did not respond. If negative, reasons behind the response were collected. If positive, methods used to share IPD were recorded. RESULTS: Across the two studies, 391 completed trials were identified. Email addresses for researchers were found for 313 (80%) of the trials. One hundred and forty-eight (47%) researchers did not respond despite being sent multiple emails. Following contact, positive initial responses were received from 92 researchers, resulting in IPD being shared for 78 trials. Eighty-seven (28%) researchers declined to share data; justifications were recorded. The median time from first request to accessing data in one study was 241 (IQR 383.3) days. IPD sources included: direct from researcher, via academic trial funders repository and a website requiring remote analysis of commercial data. Where data were shared, a variety of methods were used to transfer data. CONCLUSION: Sharing of IPD from trials is desirable and a requirement of many funding bodies. However, accessing IPD faces multiple challenges including refusals to share, delays in access to data and having to perform analyses on a remote website. TRIAL REGISTRATION: Not applicable. |
format | Online Article Text |
id | pubmed-7482449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-74824492020-09-18 Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine Scutt, Polly Woodhouse, Lisa J Montgomery, Alan A Bath, Philip M BMJ Open Research Methods OBJECTIVES: Meta-analysis based on individual patient data (IPD) from randomised trials is superior to using published summary data since it facilitates subgroup and multiple variable analyses. Guidelines and funders expect that researchers share IPD for bona fide analyses, but in practice, this is done variably. Here, we report the experience of obtaining IPD for two collaborative analysis studies. SETTING: Two linked studies required IPD from published randomised trials. The leading researchers for eligible trials were approached and asked to share IPD including trial characteristics, patient demographics, baseline clinical data and outcome measures. PARTICIPANTS: Participants in eligible randomised controlled trials included patients with or at risk of cognitive decline/vascular events. PRIMARY AND SECONDARY OUTCOME MEASURES: Numbers (%) of trials where the leading researcher responded favourably/negatively or did not respond. If negative, reasons behind the response were collected. If positive, methods used to share IPD were recorded. RESULTS: Across the two studies, 391 completed trials were identified. Email addresses for researchers were found for 313 (80%) of the trials. One hundred and forty-eight (47%) researchers did not respond despite being sent multiple emails. Following contact, positive initial responses were received from 92 researchers, resulting in IPD being shared for 78 trials. Eighty-seven (28%) researchers declined to share data; justifications were recorded. The median time from first request to accessing data in one study was 241 (IQR 383.3) days. IPD sources included: direct from researcher, via academic trial funders repository and a website requiring remote analysis of commercial data. Where data were shared, a variety of methods were used to transfer data. CONCLUSION: Sharing of IPD from trials is desirable and a requirement of many funding bodies. However, accessing IPD faces multiple challenges including refusals to share, delays in access to data and having to perform analyses on a remote website. TRIAL REGISTRATION: Not applicable. BMJ Publishing Group 2020-09-09 /pmc/articles/PMC7482449/ /pubmed/32912955 http://dx.doi.org/10.1136/bmjopen-2020-038765 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Research Methods Scutt, Polly Woodhouse, Lisa J Montgomery, Alan A Bath, Philip M Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title | Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title_full | Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title_fullStr | Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title_full_unstemmed | Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title_short | Data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
title_sort | data sharing: experience of accessing individual patient data from completed randomised controlled trials in vascular and cognitive medicine |
topic | Research Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482449/ https://www.ncbi.nlm.nih.gov/pubmed/32912955 http://dx.doi.org/10.1136/bmjopen-2020-038765 |
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